Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Adipocytes/cytology"'
Publikováno v:
Abdallah, B, Alzahrani, A M & Kassem, M 2018, ' Secreted Clusterin protein inhibits osteoblast differentiation of bone marrow mesenchymal stem cells by suppressing ERK1/2 signaling pathway ', Bone, vol. 110, pp. 221-229 . https://doi.org/10.1016/j.bone.2018.02.018
Secreted Clusterin (sCLU, also known as Apolipoprotein J) is an anti-apoptotic glycoprotein involved in the regulation of cell proliferation, lipid transport, extracellular tissue remodeling and apoptosis. sCLU is expressed and secreted by mouse bone
Publikováno v:
Journal of Lipid Research, Vol 59, Iss 7, Pp 1301-1310 (2018)
Journal of lipid research, vol. 59, no. 7, pp. 1301-1310
Journal of Lipid Research
Journal of lipid research, vol. 59, no. 7, pp. 1301-1310
Journal of Lipid Research
In vitro differentiating adipocytes are sensitive to liquid manipulations and have the tendency to float. Assessing adipocyte differentiation using current microscopy techniques involves cell staining and washing, while using flow cytometry involves
Autor:
Ronni Nielsen, Qin Yan, Søren Fisker Schmidt, Jesper Grud Skat Madsen, Ann-Sofie B. Brier, Anne Loft, Susanne Mandrup, Zongzhi Liu, Hinrich Gronemeyer, Thomas Rosengren
Publikováno v:
Brier, A-S B, Loft, A, Madsen, J G S, Nielsen, T R, Nielsen, R, Schmidt, S F, Liu, Z, Yan, Q, Gronemeyer, H & Mandrup, S 2017, ' The KDM 5 family is required for activation of pro-proliferative cell cycle genes during adipocyte differentiation ', Nucleic Acids Research, vol. 45, no. 4, pp. 1743-1759 . https://doi.org/10.1093/nar/gkw1156
Nucleic Acids Research
Nucleic Acids Research, 2017, 45 (4), pp.1743-1759. ⟨10.1093/nar/gkw1156⟩
Brier, A-S B, Loft, A, Madsen, J G S, Rosengren, T, Nielsen, R, Schmidt, S F, Liu, Z, Yan, Q, Gronemeyer, H & Mandrup, S 2017, ' The KDM5 family is required for activation of pro-proliferative cell cycle genes during adipocyte differentiation ', Nucleic Acids Research, vol. 45, no. 4, pp. 1743-1759 . https://doi.org/10.1093/nar/gkw1156
Nucleic Acids Research
Nucleic Acids Research, 2017, 45 (4), pp.1743-1759. ⟨10.1093/nar/gkw1156⟩
Brier, A-S B, Loft, A, Madsen, J G S, Rosengren, T, Nielsen, R, Schmidt, S F, Liu, Z, Yan, Q, Gronemeyer, H & Mandrup, S 2017, ' The KDM5 family is required for activation of pro-proliferative cell cycle genes during adipocyte differentiation ', Nucleic Acids Research, vol. 45, no. 4, pp. 1743-1759 . https://doi.org/10.1093/nar/gkw1156
The KDM5 family of histone demethylases removes the H3K4 tri-methylation (H3K4me3) mark frequently found at promoter regions of actively transcribed genes and is therefore generally considered to contribute to corepression. In this study, we show tha
Autor:
Brett Ba Shook, Victoria L. Seewaldt, Eve Roth, Michael C. Rudolph, Alexandra Van Keymeulen, Stephanie L. Kwei, Rachel K. Zwick, Brandon Holtrup, Matthew Ms Rodeheffer, Valerie Horsley, John J. Wysolmerski, Vivian Lei
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
Nature Communications
Nature communications, 9 (1
Nature Communications
Nature communications, 9 (1
Adipocytes undergo pronounced changes in size and behavior to support diverse tissue functions, but the mechanisms that control these changes are not well understood. Mammary gland-associated white adipose tissue (mgWAT) regresses in support of milk
Publikováno v:
Christensen, L P & El-Houri, R B 2018, ' Development of an in vitro screening platform for the identification of partial PPARγ agonists as a source for antidiabetic lead compounds ', Molecules, vol. 23, no. 10, 2431 . https://doi.org/10.3390/molecules23102431
Molecules, Vol 23, Iss 10, p 2431 (2018)
Christensen, L P & El-Houri, R 2018, ' Development of an in vitro screening platform for the identification of partial PPARγ agonists as a source for antidiabetic lead compounds ', Molecules, vol. 23, no. 10, pp. 2431 . https://doi.org/10.3390/molecules23102431
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 23, Iss 10, p 2431 (2018)
Christensen, L P & El-Houri, R 2018, ' Development of an in vitro screening platform for the identification of partial PPARγ agonists as a source for antidiabetic lead compounds ', Molecules, vol. 23, no. 10, pp. 2431 . https://doi.org/10.3390/molecules23102431
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Type 2 diabetes (T2D) is a metabolic disorder where insulin-sensitive tissues show reduced sensitivity towards insulin and a decreased glucose uptake (GU), which leads to hyperglycaemia. Peroxisome proliferator-activated receptor (PPAR)γ plays an im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55705887b450f9db5781d945f84f39e6
https://vbn.aau.dk/ws/files/287290382/Molecules_2018_23_10_2431.pdf
https://vbn.aau.dk/ws/files/287290382/Molecules_2018_23_10_2431.pdf
Autor:
Matsumura, Y., Nakaki, R., Inagaki, T., Yoshida, A., Kano, Y., Kimura, Hiroshi, Tanaka, T., Tsutsumi, S., Nakao, M., Doi, T., Fukami, K., Osborne, T. F., Kodama, T., Aburatani, H., Sakai, J.
Publikováno v:
Molecular Cell. 60:584-596
Bivalent H3K4me3 and H3K27me3 chromatin domains in embryonic stem cells keep active developmental regulatory genes expressed at very low levels and poised for activation. Here, we show an alternative and previously unknown bivalent modified histone s
Autor:
Lukas Varga, Pirjo Nuutila, Wenfei Sun, Sven Enerbäck, Patrik Stefanicka, Christian Wolfrum, Walter Wahli, Bettina Tall, Nicola Zamboni, Kirsi A. Virtanen, Elke Kiehlmann, Petra Krznar, Ez-Zoubir Amri, Lennart Opitz, Jozef Ukropec, Miroslav Balaz, Matthias Rosenwald, Martin E. Lidell, David Lasar
Publikováno v:
Cell Reports, Vol 22, Iss 3, Pp 760-773 (2018)
Cell reports, vol. 22, no. 3, pp. 760-773
Cell Reports
Cell Reports, Elsevier Inc, 2018, 22 (3), pp.760-773. ⟨10.1016/j.celrep.2017.12.067⟩
Cell reports, vol. 22, no. 3, pp. 760-773
Cell Reports
Cell Reports, Elsevier Inc, 2018, 22 (3), pp.760-773. ⟨10.1016/j.celrep.2017.12.067⟩
Peroxisome proliferator-activated receptors (PPARs) have been suggested as the master regulators of adipose tissue formation. However, their role in regulating brown fat functionality has not been resolved. To address this question, we generated mice
Autor:
Sheila M. O'Byrne, William S. Blaner, Manabu Takahashi, Konstantinos Drosatos, Yunying Hu, Ni Huiping Son, Ira J. Goldberg, Itsaso Garcia-Arcos, Yaeko Hiyama, Chuchun L. Chang, Richard J. Deckelbaum, Joseph C. Obunike, Kalyani G. Bharadwaj, Marit Westerterp, Hongfeng Jiang, Hiroaki Yagyu
Publikováno v:
The Journal of Biological Chemistry, 288(20), 14046-14058. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Journal of biological chemistry, 288(20), 14046-14058. American Society for Biochemistry and Molecular Biology Inc.
Journal of biological chemistry, 288(20), 14046-14058. American Society for Biochemistry and Molecular Biology Inc.
Adipose fat storage is thought to require uptake of circulating triglyceride (TG)-derived fatty acids via lipoprotein lipase (LpL). To determine how LpL affects the biology of adipose tissue, we created adipose-specific LpL knock-out (ATLO) mice, and
Autor:
Otani, Y., Nakatsu, Y., Sakoda, H., Fukushima, Toshiaki, Fujishiro, M., Kushiyama, A., Okubo, H., Tsuchiya, Y., Ohno, H., Takahashi, S., Nishimura, F., Kamata, H., Katagiri, H., Asano, T.
Publikováno v:
Biochemical and Biophysical Research Communications. 434:197-202
The dynamic process of adipose differentiation involves stepwise expressions of transcription factors and proteins specific to the mature fat cell phenotype. In this study, it was revealed that expression levels of IntS6 and IntS11, subunits of the I
Autor:
Vincent Bertholet, José Remacle, Paul Holvoet, Catherine Demazy, Françoise de Longueville, Silvia Tejerina, Sébastien Vankoningsloo, Martine Raes, Thierry Arnould, Patricia Renard, Andrée Houbion, Aurélia De Pauw
Publikováno v:
Journal of cell science, Vol. 119, no. Pt 7, p. 1266-82 (2006)
Several mitochondrial pathologies are characterized by lipid redistribution and microvesicular cell phenotypes resulting from triglyceride accumulation in lipid-metabolizing tissues. However, the molecular mechanisms underlying abnormal fat distribut